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Revista Mexicana de Medicina Transfusional

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Órgano oficial de la Asociación Mexicana de Medicina Transfusional A.C.
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2024, Number S1

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Rev Mex Med Transfus 2024; 16 (S1)

Uso de la biología computacional para comparar las estructuras terciarias teóricas de las formas más comunes de RHCE y RHD

Estrada JH
Full text How to cite this article 10.35366/117579

DOI

DOI: 10.35366/117579
URL: https://dx.doi.org/10.35366/117579

Language: Spanish
References: 15
Page: s10-13
PDF size: 221.78 Kb.


Key words:

No keywords




REFERENCES

  1. Zhang Y. Progress and challenges in protein structure prediction. Curr Opin Struct Biol. 2008; 18: 342-348.

  2. Conroy MJ, Bullough PA, Merrick M, Avent ND. Modelling the human rhesus proteins: implications for structure and function. Br J Haematol. 2005; 131: 543-551.

  3. Floch A, Pirenne F, Barrault A, Chami B, Toly-Ndour C, Tournamille C et al. Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions. Transfusion. 2021; 61: 1286-1301.

  4. Gruswitz F, Chaudhary S, Ho JD, Schlessinger A, Pezeshki B, Ho CM, et al. Function of human Rh based on structure of RhCG at 2.1 A. Proc Natl Acad Sci U S A. 2010; 107: 9638-9643.

  5. Zhang X, Li G, Zhou Z, Shao C, Huang X, Li L et al. Molecular and computational analysis of 45 samples with a serologic weak D phenotype detected among 132,479 blood donors in northeast China. J Transl Med. 2019; 17: 393.

  6. Trueba-Gomez R, Rosenfeld-Mann F, Estrada-Juarez H. Prediction of the antigenic regions in eight RhD variants identified by computational biology. Vox Sang. 2024; 119: 590-597.

  7. Cherif-Zahar B, Bloy C, Le Van-Kim C, Blanchard D, Bailly P, Hermand P et al. Molecular cloning and protein structure of a human blood group Rh polypeptide. Proc Natl Acad Sci U S A. 1990; 87: 6243-6247.

  8. Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Molecular basis of weak D phenotypes. Blood. 1999; 93: 385-393.

  9. Meireles MR, Stelmach LH, Bandinelli E, Vieira GF. Unveiling the influence of factor VIII physicochemical properties on hemophilia A phenotype through an in silico methodology. Comput Methods Programs Biomed. 2022; 219: 106768.

  10. Wagner FF, Ladewig B, Flegel WA. The RHCE allele ceRT: D epitope 6 expression does not require D-specific amino acids. Transfusion. 2003; 43: 1248-1254.

  11. Chen Q, Hustinx H, Flegel WA. The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids. Transfusion. 2006; 46: 766-772.

  12. Trueba-Gomez R, Rosenfeld-Mann F, Baptista-Gonzalez HA, Dominguez-Lopez ML, Estrada-Juarez H. Use of computational biology to compare the theoretical tertiary structures of the most common forms of RhCE and RhD. Vox Sang. 2023; 118: 881-890.

  13. Floch A, Galochkina T, Pirenne F, Tournamille C, de Brevern AG. Molecular dynamics of the human RhD and RhAG blood group proteins. Front Chem. 2024; 12: 1360392.

  14. Vallese F, Kim K, Yen LY, Johnston JD, Noble AJ, Cali T et al. Architecture of the human erythrocyte ankyrin-1 complex. Nat Struct Mol Biol. 2022; 29: 706-718.

  15. Nicolas V, Le Van Kim C, Gane P, Birkenmeier C, Cartron JP, Colin Y et al. Rh-RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null)-associated mutation. J Biol Chem. 2003; 278: 25526-25533.




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Rev Mex Med Transfus. 2024;16